A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124833



Internal ID21401745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133375291..133375291hg38UCSC Ensembl
chr5:132710983..132710983hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632027
Supporting Variants
SamplesHG00096
Known GenesFSTL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124833
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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